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osteoblastoma - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

osteoblastoma

MONDO:0018936

Also known as:giant osteoid osteomaossifying giant cell tumorossifying giant cell tumour

Overview

A rare benign bone-forming neoplasm usually arising from the spine. It is a well-circumscribed lytic tumor that varies in size. The tumor is composed of woven bone trabeculae and shares similar histologic characteristics with the osteoid osteoma. Surgical curettage is the treatment of choice. The prognosis is excellent.

Diagnosis

Biomarker and diagnostic research for osteoblastoma has been reported in the published literature.

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for osteoblastoma.

79 publications have been identified in PubMed for osteoblastoma. Research spans Case Report / Case Series (54%), Review / Meta-Analysis (24%), and Basic Science / Preclinical (8%).

Research Type	Count	% of Total
Patient case studies	42	54%

Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 4:28 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:58040

GARD

Genetic and Rare Diseases Info Center

GARD:18854

Questions for Your Care Team

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osteoblastoma

Overview

Diagnosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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